Structured Summary
Abstract
A condition marked by progressive CEREBELLAR ATAXIA combined with MYOCLONUS usually presenting in the third decade of life or later. Additional clinical features may include generalized and focal SEIZURES, spasticity, and DYSKINESIAS. Autosomal recessive and autosomal dominant patterns of inheritance have been reported. Pathologically, the dentate nucleus and brachium conjunctivum of the CEREBELLUM are atrophic, with variable involvement of the spinal cord, cerebellar cortex, and basal ganglia. (From Joynt, Clinical Neurology, 1991, Ch37, pp60-1)
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Classification
Broader headings
Related Concepts
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MeSH Record
Synonyms
27 entry terms
- Cerebellar Dyssynergia
- Dentate Cerebellar Ataxia
- Dentate Cerebellar Atrophy
- Dentate Nucleus Syndrome, Ramsay Hunt
- Dyssynergia Cerebellaris Myoclonica
- Dyssynergia Cerebellaris Progressiva
- Ramsay Hunt Cerebellar Syndrome
- Ramsay Hunt Dentate Syndrome
- Ataxia, Dentate Cerebellar
- Ataxias, Dentate Cerebellar
- Atrophies, Dentate Cerebellar
- Atrophy, Dentate Cerebellar
- Cerebellar Ataxias, Dentate
- Cerebellar Atrophy, Dentate
- Cerebellar Dyssynergia, Myoclonic
- Cerebellar Dyssynergias
- Cerebellar Dyssynergias, Myoclonic
- Dentate Cerebellar Ataxias
- Dentate Cerebellar Atrophies
- Dyssynergia, Cerebellar
- Dyssynergia, Myoclonic Cerebellar
- Dyssynergias, Cerebellar
- Dyssynergias, Myoclonic Cerebellar
- Myoclonic Cerebellar Dyssynergias
- Cerebelloparenchymal Disorder V
- Dyssynergia Cerebellaris Myoclonica Of Hunt
- Spinodentate Atrophy
MeSH Record
Aspects Covered
35 allowable subheadings
Indexed with the subheadings blood, cerebrospinal fluid, chemically induced, classification, complications, congenital, diagnosis, diagnostic imaging, diet therapy, drug therapy, economics, embryology, enzymology, epidemiology, ethnology, etiology, genetics, history, immunology, metabolism, microbiology, mortality, nursing, parasitology, pathology, physiopathology, prevention & control, psychology, radiotherapy, rehabilitation, surgery, therapy, urine, veterinary, virology.
MeSH Record
Indexing Annotation
do not confuse entry term RAMSAY HUNT CEREBELLAR SYNDROME with RAMSAY HUNT AURICULAR SYNDROME see HERPES ZOSTER OTICUS or RAMSAY HUNT PARALYSIS SYNDROME see PARKINSONIAN DISORDERS
MeSH Record
History Note
2000(1970); use CEREBELLAR ATAXIA 1970-1990
MeSH Record
Previous Indexing
- Cerebellar Diseases (1966-1969)
MeSH Hierarchy
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AMA Style
References
- National Library of Medicine. Myoclonic Cerebellar Dyssynergia. Medical Subject Headings (MeSH). 2026. Unique ID D002527. http://id.nlm.nih.gov/mesh/2026/D002527
- Myoclonic Cerebellar Dyssynergia. In: Wikipedia. https://en.wikipedia.org/wiki/Ramsay_Hunt_syndrome_type_1
- Myoclonic Cerebellar Dyssynergia. In: Wikidata. https://www.wikidata.org/wiki/Q3961686